Mineral Lip Balm SPF-15

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Mineral Lip Balm SPF-15
Generic name: ZINC OXIDE
Manufacturer: TUBBY TODD
Product type: HUMAN OTC DRUG
SPL set ID: 4d938672-5302-4e47-a582-c3e6467008cb
SPL ID: 29921ec7-3ef5-c018-e063-6294a90af3ef
Version: 9
Effective date: 2024-12-18
Source export date: 2026-10-27
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/2eee27992d1f29d82f827fd5be42f1314ed39ce4c497af5d81435ac6656a0957/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:22:31

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M020	openfda.application_number
brand name		Mineral Lip Balm SPF-15	openfda.brand_name
generic name		ZINC OXIDE	openfda.generic_name
manufacturer name		TUBBY TODD	openfda.manufacturer_name
ndc	package	73088-105-11	openfda.package_ndc
ndc	product	73088-105	openfda.product_ndc
ndc11	package	73088010511	derived:openfda.package_ndc
spl id		29921ec7-3ef5-c018-e063-6294a90af3ef	id
spl set id		4d938672-5302-4e47-a582-c3e6467008cb	set_id
unii		SOI2LOH54Z	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Stop use and ask a doctor if rash occurs Keep out of reach of children. If amount greater than normal use is swallowed get medical attention or call Poison Control Center immediately. • Stop use and ask a doctor if rash occurs • Stop use and ask a doctor if rash occurs

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.